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16. Genetic relationship between the Zellweger syndrome and other peroxisomal disorders characterized by an impairment in the assembly of peroxisomes. Tager JM; Brul S; Wiemer EA; Strijland A; Van Driel R; Schutgens RB; Van den Bosch H; Wanders RJ; Westerveld A Prog Clin Biol Res; 1990; 321():545-58. PubMed ID: 2183242 [TBL] [Abstract][Full Text] [Related]
17. [Phenotype--genotype relationships in peroxisome biogenesis disorders]. Shimozawa N No To Shinkei; 2001 May; 53(5):411-20. PubMed ID: 11424351 [No Abstract] [Full Text] [Related]
18. Chondrodysplasia punctatas and the peroxisomopathies: overlapping syndrome communities. Wilson GN; Holmes RD; Hajra AK Pathol Immunopathol Res; 1988; 7(1-2):113-8. PubMed ID: 3065763 [No Abstract] [Full Text] [Related]
19. Plasmalogen biosynthesis in the diagnosis of peroxisomal disorders. Kremser K; Roscher A J Clin Chem Clin Biochem; 1989 May; 27(5):315-7. PubMed ID: 2760566 [TBL] [Abstract][Full Text] [Related]
20. Very large peroxisomes in distinct peroxisomal disorders (rhizomelic chondrodysplasia punctata and acyl-CoA oxidase deficiency): novel data. De Craemer D; Zweens MJ; Lyonnet S; Wanders RJ; Poll-The BT; Schutgens RB; Waelkens JJ; Saudubray JM; Roels F Virchows Arch A Pathol Anat Histopathol; 1991; 419(6):523-5. PubMed ID: 1750197 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]